Canonical Allele Identifier: CA388569270
Gene: ERCC5 HGNC NCBI
BIVM-ERCC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.102856066A>C , CM000675.2:g.102856066A>C GRCh38
NC_000013.10:g.103508416A>C , CM000675.1:g.103508416A>C GRCh37
NC_000013.9:g.102306417A>C NCBI36
NG_007146.1:g.15243A>C , LRG_464:g.15243A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682632.1:n.723A>C (ERCC5)
ENST00000682869.1:n.1131A>C (ERCC5)
ENST00000683246.1:n.1259A>C (ERCC5)
ENST00000684184.1:n.1128A>C (ERCC5)
ENST00000638434.1:c.580A>C (BIVM-ERCC5)
ENST00000639132.1:c.1157A>C (BIVM-ERCC5) ENSP00000492684.1:p.Asp386Ala
ENST00000639435.1:c.1844A>C (BIVM-ERCC5) ENSP00000491742.1:p.Asp615Ala
ENST00000651002.1:c.*243A>C (ERCC5) ENSP00000498809.1:n.*243A>C
ENST00000651055.1:n.611A>C (ERCC5)
ENST00000651281.1:n.850A>C (ERCC5)
ENST00000651470.1:c.482A>C (ERCC5) ENSP00000498701.1:p.Asp161Ala
ENST00000652225.2:c.482A>C (ERCC5) MANE Select ENSP00000498881.2:p.Asp161Ala
ENST00000652613.1:c.-23A>C (ERCC5) ENSP00000498357.1:n.-23A>C
ENST00000355739.8:c.482A>C (ERCC5) ENSP00000347978.4:p.Asp161Ala
ENST00000535557.5:c.482A>C (ERCC5) ENSP00000442117.1:p.Asp161Ala
ENST00000602836.1:c.1758A>C (BIVM-ERCC5)
ENST00000610537.4:c.482A>C (ERCC5) ENSP00000478667.1:p.Asp161Ala
NM_000123.3:c.482A>C , LRG_464t1:c.482A>C (ERCC5) NP_000114.2:p.Asp161Ala
NM_001204425.1:c.1844A>C (BIVM-ERCC5) NP_001191354.1:p.Asp615Ala
NM_000123.4:c.482A>C (ERCC5) MANE Select NP_000114.3:p.Asp161Ala
NM_001204425.2:c.1844A>C (BIVM-ERCC5) NP_001191354.2:p.Asp615Ala